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1.
Functional and genetic epidemiological characterisation of the FFAR4 (GPR120) p.R270H variant in the Danish population.
J Med Genet
; 53(9): 616-23, 2016 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-27068006
2.
Increasing insulin resistance accentuates the effect of triglyceride-associated loci on serum triglycerides during 5 years.
J Lipid Res
; 57(12): 2193-2199, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27777317
3.
The Arg82Cys Polymorphism of the Protein Nepmucin Implies a Role in HDL Metabolism.
J Endocr Soc
; 6(5): bvac034, 2022 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35382499
4.
Indirect comparison of efficacy of dupilumab versus mepolizumab and omalizumab for severe type 2 asthma.
ERJ Open Res
; 7(3)2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34476242
5.
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).
BMC Med Genet
; 11: 42, 2010 Mar 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-20226046
6.
Efficacy of omalizumab in children, adolescents, and adults with severe allergic asthma: a systematic review, meta-analysis, and call for new trials using current guidelines for assessment of severe asthma.
Allergy Asthma Clin Immunol
; 16: 49, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32565844
7.
Efficacy, adverse events, and inter-drug comparison of mepolizumab and reslizumab anti-IL-5 treatments of severe asthma - a systematic review and meta-analysis.
Eur Clin Respir J
; 5(1): 1536097, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30533206
8.
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Nat Commun
; 9(1): 321, 2018 01 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-29358691
9.
Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Nat Commun
; 9(1): 2162, 2018 05 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-29849136
10.
Type 2 diabetes risk alleles near BCAR1 and in ANK1 associate with decreased ß-cell function whereas risk alleles near ANKRD55 and GRB14 associate with decreased insulin sensitivity in the Danish Inter99 cohort.
J Clin Endocrinol Metab
; 98(4): E801-6, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23457408
11.
Genetic risk score of 46 type 2 diabetes risk variants associates with changes in plasma glucose and estimates of pancreatic ß-cell function over 5 years of follow-up.
Diabetes
; 62(10): 3610-7, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23835328
12.
The birth weight lowering C-allele of rs900400 near LEKR1 and CCNL1 associates with elevated insulin release following an oral glucose challenge.
PLoS One
; 6(11): e27096, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-22073261
13.
Do gene variants influencing adult adiposity affect birth weight? A population-based study of 24 loci in 4,744 Danish individuals.
PLoS One
; 5(12): e14190, 2010 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21152014
14.
MTNR1B G24E variant associates With BMI and fasting plasma glucose in the general population in studies of 22,142 Europeans.
Diabetes
; 59(6): 1539-48, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20200315
15.
Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes.
Eur J Endocrinol
; 160(4): 603-9, 2009 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19147600
16.
Association of variants in the sterol regulatory element-binding factor 1 (SREBF1) gene with type 2 diabetes, glycemia, and insulin resistance: a study of 15,734 Danish subjects.
Diabetes
; 57(4): 1136-42, 2008 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-18192539
17.
Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies.
Diabetes
; 56(12): 3105-11, 2007 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-17827400
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